Medical Information Technology, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1365-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.

Product Classification:

Class II

Date Initiated: May 7, 2013

Date Posted: May 29, 2013

Recall Number: Z-1365-2013

Event ID: 65158

Reason for Recall:

Incorrect transmission of laboratory results.

Status: Terminated

Product Quantity: 56 devices

Code Information:

Magic Releases 5.41, 5.52. 5.53, 5.62, 5.63, 5.64 and Client Server Releases 5.64, 5.65, 6.05, 6.06, 6.07

Distribution Pattern:

Worldwide Distribution - USA, including Puerto Rico and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated